US2567930A - Preparation of epoxy compounds by oxidation of cis-monoolefine compounds - Google Patents
Preparation of epoxy compounds by oxidation of cis-monoolefine compounds Download PDFInfo
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- US2567930A US2567930A US575316A US57531645A US2567930A US 2567930 A US2567930 A US 2567930A US 575316 A US575316 A US 575316A US 57531645 A US57531645 A US 57531645A US 2567930 A US2567930 A US 2567930A
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D303/00—Compounds containing three-membered rings having one oxygen atom as the only ring hetero atom
- C07D303/02—Compounds containing oxirane rings
- C07D303/38—Compounds containing oxirane rings with hydrocarbon radicals, substituted by carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D303/00—Compounds containing three-membered rings having one oxygen atom as the only ring hetero atom
- C07D303/02—Compounds containing oxirane rings
- C07D303/04—Compounds containing oxirane rings containing only hydrogen and carbon atoms in addition to the ring oxygen atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D303/00—Compounds containing three-membered rings having one oxygen atom as the only ring hetero atom
- C07D303/02—Compounds containing oxirane rings
- C07D303/12—Compounds containing oxirane rings with hydrocarbon radicals, substituted by singly or doubly bound oxygen atoms
- C07D303/14—Compounds containing oxirane rings with hydrocarbon radicals, substituted by singly or doubly bound oxygen atoms by free hydroxyl radicals
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D303/00—Compounds containing three-membered rings having one oxygen atom as the only ring hetero atom
- C07D303/02—Compounds containing oxirane rings
- C07D303/38—Compounds containing oxirane rings with hydrocarbon radicals, substituted by carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
- C07D303/40—Compounds containing oxirane rings with hydrocarbon radicals, substituted by carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals by ester radicals
- C07D303/42—Acyclic compounds having a chain of seven or more carbon atoms, e.g. epoxidised fats
Definitions
- This invention relates to the oxidation of unsaturated materials, and more particularly to a process for the preparation of epoxy compounds by oxidizing straight-chain aliphatic cis-monoolefine compounds, such as cis-monoolefines, cismonooleflne acids, esters of such acids, cis-monoolefine alcohols, etc., containing more than four carbon atoms, with aliphatic per-acids, such as peracetic, perbutyric, etc., dissolved in acidsolution, such as acetic acid.
- Such epoxy compounds are useful as chemical intermediates in organic synthesis and in the preparation of plastics, rubber-like materials, etc.
- the cis-monoolefine compounds applicable to the inventionv include, among others, such cis-monoolefine acids as oleic, ricinoleic, undecylenic, palmitoleic, petroselinic, vaccenic, erucic, etc.; the esters of these acids; the amylenes; cis-monoolefine alcohols, such as selachyl alcohol, the decenols, tetradecenols, hexadecenols, etc.; synthetic monoglycerides, such as glycerol monooleate and glycerol monoricinoleate, and others.
- Example I To 77 cc. of a well stirred glacial acetic acid solution containing 0.0735 mole of peracetic acid at room temperature is added 17.5 g. (0.062 mole) of oleic acid. The reaction is exothermic and requires cooling.
- Example II Using the same reaction procedure as described in Example I; 10 g. of methyl oleate is oxidized for about 3 hours with 32 cc. of a glacial acetic acid solution containing 0.0366 mole of peracetic acid.
- Example IV Example V Using the same reaction procedure as described in Example I, 50 g. of methyl 10,11-hendecenoate The ether aae'aeso (methyl undecylenate) is oxidized for about 24 hours with 351 cc. of a glacial acetic acid solution containing 0.365 mole of peracetic acid.
- a process comprising oxidizing oleic acid with peracetic acid dissolved in' acetic acid at room temperature for about two hours, then mixing the reaction mixture with ice water, and then isolating the formed precipitate, which comprises mainly 9,10-epoxystearic acid, from the resulting aqueous solution.
- a process comprising mixing a straightchain aliphatic cis-monooleflne compound containing more than four carbon atoms with an aliphatic per-acid selected from the group consisting of peracetic acid and perbutyric acid, respectively, in an organic acid solution of the corresponding aliphatic carboxylic acid to break the double bond of the monooleflne compound and add oxygen thereto to form an epoxy compound without otherwise altering the molecular structure of the monoolefine compound, and isolating the formed epoxy compound.
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- Organic Chemistry (AREA)
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Description
Patented Sept. 18, 1951 2,567,930 I PREPARATION OF EPOXY COMPOUNDS BY OXIDATION OF CIS-MONOOLEFINE COM- POUNDS Thomas W. Findley and Daniel Swern, Phiiadelphia, Pa., assignors to the United States of America, as represented by the Secretary of Agriculture No Drawing.
Application January 30, 1945, Serial No. 575,316
8 Claims. (Cl. 260348.5)
(Granted under the act of March 3, 1883, as
amended April 30, 1928; 370 0. G. 757) This application is made under the act of March 3, 1883, as amended by the act of April 30, 1928, and the invention herein described, if patented, may be manufactured and used by or for the Government of the United States of America for governmental purposes without the payment to us of any royalty thereon.
This invention relates to the oxidation of unsaturated materials, and more particularly to a process for the preparation of epoxy compounds by oxidizing straight-chain aliphatic cis-monoolefine compounds, such as cis-monoolefines, cismonooleflne acids, esters of such acids, cis-monoolefine alcohols, etc., containing more than four carbon atoms, with aliphatic per-acids, such as peracetic, perbutyric, etc., dissolved in acidsolution, such as acetic acid. Such epoxy compounds are useful as chemical intermediates in organic synthesis and in the preparation of plastics, rubber-like materials, etc.
We have found that epoxy compounds may be prepared directly in good yield by the oxidation of straight-chain aliphatic cis-monoolefine compounds containing more than four carbon atoms with aliphatic per-acids, such as peracetic, perbutyric acid, etc., in an organic acid solution of the corresponding aliphatic carboxylic acid, such as acetic acid, butyric acid, etc., by proper regulation of the reaction conditions. In the reaction the double bond of themonoolefine compound is broken and oxygen is added thereto to form the epoxy compound without otherwise altering the molecular structure of the monoolefine compound. The cis-monoolefine compounds applicable to the inventionv include, among others, such cis-monoolefine acids as oleic, ricinoleic, undecylenic, palmitoleic, petroselinic, vaccenic, erucic, etc.; the esters of these acids; the amylenes; cis-monoolefine alcohols, such as selachyl alcohol, the decenols, tetradecenols, hexadecenols, etc.; synthetic monoglycerides, such as glycerol monooleate and glycerol monoricinoleate, and others.
The following examples are illustrative of the invention.
Example I To 77 cc. of a well stirred glacial acetic acid solution containing 0.0735 mole of peracetic acid at room temperature is added 17.5 g. (0.062 mole) of oleic acid. The reaction is exothermic and requires cooling.
After about 2 hours at room temperature, the reaction mixture is poured into ice water,this aqueous solution flltered and the precipitate washed free from acetic acid. The precipitate is then dried, yielding 17.2 g. of a product comprising 9,10-epoxystearic acid mainly. The neutralization equivalent which was calculated to be 298.5 was found to be 298. The epoxy oxygen calculated to be 5.36% was found to be 4.6%. Recrystallization from acetone gave 12.0 g. of 9,10-epoxystearic acid having a melting point of about from 58.5 C. to 592 C.
Example II Using the same reaction procedure as described in Example I; 10 g. of methyl oleate is oxidized for about 3 hours with 32 cc. of a glacial acetic acid solution containing 0.0366 mole of peracetic acid.
The solution is then poured into cold water and the oil obtained is separated from the aqueous solution and dissolved in ether. solution is then washed free of entrained acid and dried. Evaporation of the ether yields 9.7 g. of product comprising methyl 9,10-epoxystearate mainly. The epoxy oxygen which was calculated to be 5.12% was found to be 4.5%.
Example III stantially pure 9,10-epoxyoctadecanol, having a melting point of about 52.5" C. to 54 C. This compound is claimed in an applicationfiled December 8, 1944, Serial No. 567,297, now Patent'No. 2,411,762, issued November 26, 1946.
Example IV Example V Using the same reaction procedure as described in Example I, 50 g. of methyl 10,11-hendecenoate The ether aae'aeso (methyl undecylenate) is oxidized for about 24 hours with 351 cc. of a glacial acetic acid solution containing 0.365 mole of peracetic acid.
The solution is then poured into cold water and the oil obtained is separated, as described in Example II. The product is a pale-yellow oil comprising methyl 10,11-epoxyhendecanoate. The epoxy oxygen which was calculated to be 7.47% was found to be 5.23%. Fractional distillation yielded 22 g. of methyl 10,11-epoxyhendecanoate. having a boiling point of about from 87 C. to 93 C. at 0.03 mm. of mercury. The epoxy oxygen was then found to be 7.28%.
Example VI Using the same reaction procedure as described in Example I, 20 g. of mixed amylenes is oxidized for about 4 hours with 330 cc. of a glacial acetic acid solution containing 0.343 mole of peracetic acid.
The solution is poured into cold water, neutralized with 6 N aqueous sodium hydroxide and the reaction product extracted with ether. The ether solution is dried and distilled, without fractionation, to a maximum pot temperature of about 125 C. .The distillate is then redistilled through an eflicient fractionating column to a maximum pot temperature of about 85 0., yielding 3.3 g. of pot residue comprising epoxypentanes mainly. The epoxy oxygen which was calculated to be 18.2% was found to be 9.9%.
Example VII To a solution of 28.8 g. of oleic acid dissolved in 240 cc. of acetone at about 5 C. is added 42.7 cc. of acetaldehyde. This solution is blown with air for about 25 hours at about C. to C. while being irradiated at the same time with a mercury vapor lamp. Under these conditions peracetic acid is formed and utilized in situ.
Upon dilution of this solution with water and filtering, 27 g. of colorless semi-solid is obtained. Analysis reveals that this semi-solid contains about 28% of 9,10-epoxystearic acid which is then isolated by crystallization from acetone.
Example VIII A solution consisting of 28.5 g. of oleic acid and 194 g. of butyraldehyde is blown with air for about 7 hours at about 30 C. while being irradiated at the same time with a mercury vapor lamp. Under these conditions perbutyric acid is formed and utilized in situ.
Upon dilution with cold water and after filtering this aqueous solution, 27.5 g. of a semi-solid -material is obtained. Crystallization from methanol and petroleum ether yields 6.8 g. of 9,10- epoxystearic acid.
Example IX Using the same procedure as described in Example V'HI, 28.5 g. of oleic acid is oxidized for about 5 hours but no cooling is employed. The reaction is exothermic and the temperature rises rapidly to about 50 C. to 55 C. Upon crystallization, 8 g. of 9,10-epoxystearic acid is obtained.
Example X Using the same reaction procedure as described in Example V111, 28.5 8. of oleic acid is oxidized for about hours but no mercury vapor light is used. Upon crystallization, 1 g. of 9,10-epoxystearic acid is obtained.
' Example x1 Using the same procedure as described in E!- ample VII, a solution comprising 28.3 g. of oleic acid, cc. of acetone, and 88.1 cc. of butyraldehyde is blown with air at about 0 C. to 5 C. for about 25 hours.
Upon dilution with cold water and filtering this resulting solution, 26 g. of a pale-yellow semisolid is obtained. Analysis reveals that this semisolid contains 39% of 9, l0-epoxystearicacid and upon crystallization from acetone, 5 g. of 9,10- epoxystearic acid is isolated.
Although it has been found to be most convenient to operate at the temperatures given in the examples, other temperatures may be used, provided that the epoxy compounds and peracids are stable. Likewise, other solvents and photosensitizers besides acetone may be employed. The length of time required for the completion of the reaction is primarily dependent upon the olefine oxidized and the temperature. The shortest time necessary for the completion of the reaction at any particulartemperature should be used for maximum yields of epoxy compounds.
Having thus described the invention, what is claimed is:
1. A process comprising oxidizing oleic acid with peracetic acid dissolved in' acetic acid at room temperature for about two hours, then mixing the reaction mixture with ice water, and then isolating the formed precipitate, which comprises mainly 9,10-epoxystearic acid, from the resulting aqueous solution.
2. A process comprising mixing a straightchain aliphatic cis-monooleflne compound containing more than four carbon atoms with an aliphatic per-acid selected from the group consisting of peracetic acid and perbutyric acid, respectively, in an organic acid solution of the corresponding aliphatic carboxylic acid to break the double bond of the monooleflne compound and add oxygen thereto to form an epoxy compound without otherwise altering the molecular structure of the monoolefine compound, and isolating the formed epoxy compound.
3. A process comprising mixing a straightchain aliphatic cis-monoolefine compound containing more than four carbon atoms with pen-- cetic acid dissolved in acetic acid to break the double bond of the monoolefine compound and add oxygen thereto to form an epoxy compound without otherwise altering the molecular structure of the monoolefine compound, and isolating the formed epoxy compound.
4. A process comprising mixing a straightchain aliphatic cis-monoolefine acid containing more than four carbon atoms with an aliphatic per-acid selected from the group consisting of peracetic acid and perbutyric acid, respectively, in an organic solution of the corresponding aliphatic carboxylic acid to break the double bond of the monoolefine acid and add oxygen thereto to form an epoxy compound without otherwise altering the molecular structure of the monoolefine acid, and isolating the formed epoxy compound.
5. A process comprising mixing oleic acid with an aliphatic per-acid selected from the group consisting of peracetic acid and perbutyric acid. respecively, in an organic acid solution of the corresponding aliphatic carboxylic acid to break the double bond of the oleic acid and add oxygen thereto to form 9,10-epoxystearic acid, and isolating the formed 9,10-epoxystearic acid.
6. A process comprising mixing oleic acid with peracetic acid in acetic acid solution to break the double bond of the oleic acid and add oxygen thereto to form 9,10-epoxystearic acid, and isolating the formed 9,10-epoxystearic acid.
7. A process comprising passing a free-oxygencontaining gas through a solution of a straightchain aliphatic cis-monoolefine compound containing more than four carbon atoms dissolved in an aliphatic aldehyde selected from the group consisting of acetaldehyde and butyraldehyde, to break the double bond of the monooleflne compound and add oxygen thereto to form an epoxy compound without otherwise altering the molecular structure of the monoolefine compound, and isolating the formed epoxy compound.
8. A process comprising passing a free-oxygencontaining gas through a solution of a straightchain aliphatic cis-monooleflne compound containing more than four carbon atoms dissolved in an aliphatic aldehyde selected from the group consisting of acetaldehyde and butyraldehyde while exposing said solution to ultra violet radia- I tion, to break the double bond of the monoolefine compound and add oxygen thereto to form an epoxy compound without otherwise altering the molecular structure of the monooleflne compound, and isolating the formed epoxy compound.
. THOMAS W. FINDLEY.
DANIEL SWERN.
REFERENCES CITED The following references are of record in th file of this patent:
UNITED STATES PATENTS Number Name Date 1,483,546 Gelissen et al Feb. 12, 1924 2,115,206 Milas Apr. 20, 1938 2,458,484 Terry Jan. 4. 1949 OTHER REFERENCES King: J. Chem. Soc. 37 (1943). Pp. 37-38.
Gilman: Organic Chemistry An Advanced Treatise, vol. 1, second edition, pp. 634 and 635, John Wiley and Sons Inc., London, 1943.
Smit: Recueil Des Travaux Chimques Des Pays-Baas, Tome 49, pages 684 and 685.
Grant: Hackhs Chemical Dictionary, page 593, 3rd edition, Blakiston Co., Philadelphia. 1944.
Smit: articles abstracted in Chemical Abstracts, vol 24, pp. 4261-4263 (1930).
Arbuzov et al.: articles abstracted in Chemical Abstracts, vol. 24, pp. 4285-4286 (1930).
Boeseken et al.: article abstracted in Chemical Abstracts, vol. 25, page 5403 (1931).
Stuurman: article abstracted in Chemical Abstracts, vol. 29, page 4657 (1935).
Krug et al.: German Pat. No. 730,116, abstracted in Chemical Abstracts, Vol.38, page 979 (1944).
Claims (1)
1. A PROCESS COMPRISING OXIDIZING OLEIC ACID WITH PARACETIC ACID DISSOLVED IN ACETIC ACID AT ROOM TEMPERTURE FOR ABOUT TWO HOURS, THEN MIXING THE REACTION MIXTURE WITH ICE WATER, AND THEN ISOLATING THE FORMED PRECIPITATE, WHICH COMPRISES MAINLY 9,10-EPOXYSTEARIC ACID, FROM THE RESULTING AQUEOUS SOLUTION.
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| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US575316A US2567930A (en) | 1945-01-30 | 1945-01-30 | Preparation of epoxy compounds by oxidation of cis-monoolefine compounds |
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| Application Number | Priority Date | Filing Date | Title |
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| US575316A US2567930A (en) | 1945-01-30 | 1945-01-30 | Preparation of epoxy compounds by oxidation of cis-monoolefine compounds |
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| US2567930A true US2567930A (en) | 1951-09-18 |
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Cited By (20)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2745846A (en) * | 1952-01-28 | 1956-05-15 | Monsanto Chemicals | Epoxidized acyl ricinoleates |
| US2774774A (en) * | 1954-03-26 | 1956-12-18 | Fmc Corp | In situ epoxidation of oleic acid using formic acid |
| US2785185A (en) * | 1952-08-07 | 1957-03-12 | Union Carbide & Carbon Corp | Process for making oxirane compounds from olefins and aldehyde monoperacylates |
| US2801253A (en) * | 1957-07-30 | In situ epoxidation of organic esters | ||
| US2810732A (en) * | 1957-10-22 | In situ epoxidation of fatty acids | ||
| DE1019307B (en) * | 1952-08-07 | 1957-11-14 | Union Carbide Corp | Process for the preparation of epoxy compounds |
| US2813878A (en) * | 1953-01-26 | 1957-11-19 | Archer Daniels Midland Co | Method of preparing epoxidized oils and the like |
| US2822368A (en) * | 1953-07-15 | 1958-02-04 | Rohm & Haas | Epoxidized vegetable oils |
| US2900342A (en) * | 1956-12-18 | 1959-08-18 | Pure Oil Co | Lubricants |
| US2997484A (en) * | 1961-08-22 | Method of epoxidation of unsaturated | ||
| DE975394C (en) * | 1952-04-10 | 1961-11-16 | Henkel & Cie Gmbh | Process for the production of ester-like products suitable as plasticizers for plastics, in particular vinyl polymers |
| US3112325A (en) * | 1954-01-25 | 1963-11-26 | Asahi Electrochemical Ind Comp | Process for manufacture of epoxidized fatty acids, alcohols and esters thereof |
| US3129231A (en) * | 1964-04-14 | Ethylene oxide adducts of epoxy- | ||
| US3218296A (en) * | 1962-07-30 | 1965-11-16 | Tenneco Chem | Initiators for the polymerization of formaldehyde |
| US3265716A (en) * | 1963-07-09 | 1966-08-09 | Eastman Kodak Co | Epoxidation of olefins during the simultaneous air oxidation of secondary aldehydes |
| US3346473A (en) * | 1967-10-10 | Production of olefin oxides and carboxylic acids | ||
| US3347763A (en) * | 1962-07-02 | 1967-10-17 | Ici Ltd | Production of oxygen-containing organic compounds |
| US3379737A (en) * | 1963-01-03 | 1968-04-23 | Shawinigan Chem Ltd | Epoxide production |
| DE1301305B (en) * | 1962-05-02 | 1969-08-21 | Osaka Soda Co Ltd | Process for the production of propylene oxide |
| US3493631A (en) * | 1967-11-16 | 1970-02-03 | Ppg Industries Inc | Epoxidized polyesters prepared from hydrogenated bisphenols and tetrahydrophthalic acid in equimolar amounts |
Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US1483546A (en) * | 1922-12-04 | 1924-02-12 | Firm Naamlooze Vennootschap In | Process for bleaching and improving flour and milling products |
| US2115206A (en) * | 1935-04-05 | 1938-04-26 | Nicholas A Milas | Method of making organic peroxides |
| US2458484A (en) * | 1946-06-17 | 1949-01-04 | Gen Mills Inc | Process of preparing epoxy derivatives from unsaturated aliphatic compounds |
-
1945
- 1945-01-30 US US575316A patent/US2567930A/en not_active Expired - Lifetime
Patent Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US1483546A (en) * | 1922-12-04 | 1924-02-12 | Firm Naamlooze Vennootschap In | Process for bleaching and improving flour and milling products |
| US2115206A (en) * | 1935-04-05 | 1938-04-26 | Nicholas A Milas | Method of making organic peroxides |
| US2458484A (en) * | 1946-06-17 | 1949-01-04 | Gen Mills Inc | Process of preparing epoxy derivatives from unsaturated aliphatic compounds |
Cited By (20)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2997484A (en) * | 1961-08-22 | Method of epoxidation of unsaturated | ||
| US3346473A (en) * | 1967-10-10 | Production of olefin oxides and carboxylic acids | ||
| US3129231A (en) * | 1964-04-14 | Ethylene oxide adducts of epoxy- | ||
| US2801253A (en) * | 1957-07-30 | In situ epoxidation of organic esters | ||
| US2810732A (en) * | 1957-10-22 | In situ epoxidation of fatty acids | ||
| US2745846A (en) * | 1952-01-28 | 1956-05-15 | Monsanto Chemicals | Epoxidized acyl ricinoleates |
| DE975394C (en) * | 1952-04-10 | 1961-11-16 | Henkel & Cie Gmbh | Process for the production of ester-like products suitable as plasticizers for plastics, in particular vinyl polymers |
| DE1019307B (en) * | 1952-08-07 | 1957-11-14 | Union Carbide Corp | Process for the preparation of epoxy compounds |
| US2785185A (en) * | 1952-08-07 | 1957-03-12 | Union Carbide & Carbon Corp | Process for making oxirane compounds from olefins and aldehyde monoperacylates |
| US2813878A (en) * | 1953-01-26 | 1957-11-19 | Archer Daniels Midland Co | Method of preparing epoxidized oils and the like |
| US2822368A (en) * | 1953-07-15 | 1958-02-04 | Rohm & Haas | Epoxidized vegetable oils |
| US3112325A (en) * | 1954-01-25 | 1963-11-26 | Asahi Electrochemical Ind Comp | Process for manufacture of epoxidized fatty acids, alcohols and esters thereof |
| US2774774A (en) * | 1954-03-26 | 1956-12-18 | Fmc Corp | In situ epoxidation of oleic acid using formic acid |
| US2900342A (en) * | 1956-12-18 | 1959-08-18 | Pure Oil Co | Lubricants |
| DE1301305B (en) * | 1962-05-02 | 1969-08-21 | Osaka Soda Co Ltd | Process for the production of propylene oxide |
| US3347763A (en) * | 1962-07-02 | 1967-10-17 | Ici Ltd | Production of oxygen-containing organic compounds |
| US3218296A (en) * | 1962-07-30 | 1965-11-16 | Tenneco Chem | Initiators for the polymerization of formaldehyde |
| US3379737A (en) * | 1963-01-03 | 1968-04-23 | Shawinigan Chem Ltd | Epoxide production |
| US3265716A (en) * | 1963-07-09 | 1966-08-09 | Eastman Kodak Co | Epoxidation of olefins during the simultaneous air oxidation of secondary aldehydes |
| US3493631A (en) * | 1967-11-16 | 1970-02-03 | Ppg Industries Inc | Epoxidized polyesters prepared from hydrogenated bisphenols and tetrahydrophthalic acid in equimolar amounts |
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